Yamamoto Motohisa, Takahashi Hiroki, Miyamoto Chie, Ohara Mikiko, Suzuki Chisako, Naishiro Yasuyoshi, Yamamoto Hiroyuki, Shinomura Yasuhisa, Nonaka Michio, Imai Kohzoh
First Department of Internal Medicine, Sapporo Medical University School of Medicine.
Nihon Rinsho Meneki Gakkai Kaishi. 2006 Jun;29(3):160-8. doi: 10.2177/jsci.29.160.
The subject was a 22-year-old woman who developed high fever and arthralgias and eruptions in the extremities around June 2005. She sought medical advice at a nearby dermatology clinic, where hepatic dysfunction was noted on blood testing. The patient was thus hospitalized the next day. Although CRP levels were significantly high, no sign of infection was observed and bone marrow cell differentiation was normal. Adult onset Still's disease was diagnosed based on the observation of persistent high fever >39 degrees C, eruptions, increased leukocytes, pharyngeal pain, splenomegaly, hepatic dysfunction, negative autoantibody results from blood testing, and high serum ferritin levels. Administration of prednisolone 30 mg/day was initiated, but proved ineffective. Steroid pulse therapy was conducted, and the subject was transferred to our medical facility for continued treatment. Attempts were made to control the disease using combined steroid and cyclosporine administration; but exacerbation of high serum ferritin levels and hepatic dysfunctions were observed, so a second course of steroid pulse therapy was conducted. Symptoms improved temporarily, but steroid levels were difficult to reduce. Cyclosporine was therefore replaced by methotrexate, and administration of infliximab was initiated. In the course of treatment, administration of a sulfamethoxazole/trimethoprim combination was initiated, but was discontinued due to suspicion of drug-induced hepatic injury. A second administration of infliximab was conducted in late August, and rapid improvements in clinical symptoms and abnormal test values was observed. However, high fever and headache developed suddenly in early September. Based on the results of spinal fluid testing, blood and spinal fluid cultures and MRI of the head, Listeria meningoencephalitis was diagnosed. Diplopia and impaired consciousness occurred during the disease course, and formation of a brain abscess was observed on imaging. However, symptoms were controlled by long-term combination administration of ampicillin and gentamicin. Administration of infliximab was discontinued for treatment of adult onset Still's disease, and steroid levels were reduced following double-membrane filtration plasma exchange. On follow-up, no relapse of symptoms or abnormalities in blood test values were observed, so the subject was discharged from our medical facility in December 2005. In treatment for rheumatic diseases, a dramatic improvement in treatment results for pathologies displaying tolerance against conventional treatments has been acquired with the development of biological drugs. However, opportunistic infections represent a serious problem, and appropriate preventative measures are required. The present report describes a case in which the subject was affected by Listeria meningoencephalitis during administration of infliximab for steroid-dependent adult Still's disease. Since listeriosis is one of the complications, along with tuberculosis, that warrants precautionary measures, this case is reported and discussed.
患者为一名22岁女性,2005年6月左右出现高热、关节痛及四肢皮疹。她在附近的皮肤科诊所就医,血液检查发现肝功能异常。患者于次日住院。尽管CRP水平显著升高,但未观察到感染迹象,骨髓细胞分化正常。根据持续高热>39℃、皮疹、白细胞增多、咽痛、脾肿大、肝功能异常、血液检查自身抗体结果阴性及血清铁蛋白水平升高,诊断为成人斯蒂尔病。开始每日给予30mg泼尼松龙治疗,但无效。进行了类固醇冲击疗法,患者被转至我院继续治疗。尝试联合使用类固醇和环孢素控制病情,但观察到血清铁蛋白水平升高和肝功能恶化,因此进行了第二个疗程的类固醇冲击疗法。症状暂时改善,但类固醇水平难以降低。因此将环孢素换成甲氨蝶呤,并开始使用英夫利昔单抗。在治疗过程中,开始使用磺胺甲恶唑/甲氧苄啶联合用药,但因怀疑药物性肝损伤而停药。8月底再次给予英夫利昔单抗,临床症状和异常检查值迅速改善。然而,9月初突然出现高热和头痛。根据脑脊液检查、血液和脑脊液培养及头部MRI结果,诊断为李斯特菌性脑膜脑炎。病程中出现复视和意识障碍,影像学检查发现脑脓肿形成。然而,通过长期联合使用氨苄西林和庆大霉素,症状得到控制。因治疗成人斯蒂尔病停用英夫利昔单抗,经双重膜过滤血浆置换后类固醇水平降低。随访时,未观察到症状复发或血液检查值异常,因此患者于2005年12月从我院出院。在风湿性疾病的治疗中,随着生物药物的发展,对传统治疗耐药的疾病的治疗效果有了显著改善。然而,机会性感染是一个严重问题,需要采取适当的预防措施。本报告描述了一例在使用英夫利昔单抗治疗类固醇依赖型成人斯蒂尔病期间发生李斯特菌性脑膜脑炎患者的病例。由于李斯特菌病是需要采取预防措施的并发症之一,与结核病一样,故报告并讨论此病例。